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Use of cyclodextrins for manipulating cellular cholesterol content

Open access
Christian, A E, Haynes, M P, Phillips, M C, Rothblat, G H·1997·Journal of Lipid Research

Abstract

Previous studies from this laboratory have demonstrated that exposure of tissue culture cells to cyclodextrins results in rapid cholesterol depletion. In the present study, we have developed experimental systems for using solutions of cyclodextrins, either 2-hydroxypropyl beta-cyclodextrin or methylated beta-cyclodextrin, complexed with varying amounts of free cholesterol to manipulate cell cholesterol content. Cholesterol delivered via the cyclodextrin has been found to be metabolically active, as measured by the acyl-coenzyme A:cholesterol acyltransferase (ACAT)-mediated esterification of [3H]cholesterol in Fu5AH rat hepatoma cells and Chinese hamster ovary cells. The methylated beta-cyclodextrin was found to be a more efficient donor in all cell types studied, with an average cholesterol uptake of at least 100 microg cholesterol/mg protein within 6 h. By modifying the cyclodextrin:cholesterol molar ratio, it is possible to manipulate the cellular cholesterol content of cells, producing conditions ranging from net cholesterol enrichment to depletion. The use of cyclodextrins provides a convenient, precise and reproducible method for modulating the cholesterol content of tissue culture cells.

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Metadata

Authors
Christian, A. E., Haynes, M. P., Phillips, M. C., & Rothblat, G. H.
Venue
Journal of Lipid Research
Publisher
Elsevier BV
Published
1997-11
Volume
38
Issue
11
Pages
2264-2272
ISSN
0022-2275 (ISSN-L)
OpenAlex
W2130388575
Cited by
754
References
1
FWCI
8.17
Type
journal article
Language
en
Open access
hybrid

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CoChat. (2026). Citation check: Use of cyclodextrins for manipulating cellular cholesterol content. https://app.cochat.ai/papers/10.1016/s0022-2275(20)34940-3
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Christian, A. E., Haynes, M. P., Phillips, M. C., & Rothblat, G. H. (1997). Use of cyclodextrins for manipulating cellular cholesterol content. Journal of Lipid Research. https://doi.org/10.1016/s0022-2275(20)34940-3

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